Autosomal Dominant Pseudohypoaldosteronism Type 1 in an Infant with Salt Wasting Crisis Associated with Urinary Tract Infection and Obstructive Uropathy

Type 1 pseudohypoaldosteronism (PHA1) is a salt wasting syndrome caused by renal resistance to aldosterone. Primary renal PHA1 or autosomal dominant PHA1 is caused by mutations in mineralocorticoids receptor gene (NR3C2), while secondary PHA1 is frequently associated with urinary tract infection (UT...

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Detalles Bibliográficos
Autores principales: Bowden, Sasigarn A., Cozzi, Corin, Hickey, Scott E., Thrush, Devon Lamb, Astbury, Caroline, Nuthakki, Sushma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880733/
https://www.ncbi.nlm.nih.gov/pubmed/24455331
http://dx.doi.org/10.1155/2013/524647

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880733/
https://www.ncbi.nlm.nih.gov/pubmed/24455331
http://dx.doi.org/10.1155/2013/524647

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